Approaches to analyze the role of Rab GTPases in endocytic trafficking of epidermal growth factor receptor (EGFR).

Methods Mol Biol

Department of Biochemistry, Yong Loo Lin School of Medicine, National University of Singapore, 8 Medical Drive, Singapore, 117597, Singapore.

Published: November 2015

AI Article Synopsis

  • The epidermal growth factor receptor (EGFR) is crucial for cell signaling, influencing development and various diseases.
  • EGFR's signaling is affected by its endocytic trafficking, which is regulated by specific proteins called Rab small GTPases.
  • The chapter outlines protocols to study the role of Rab proteins, particularly Rab31, in EGFR’s endocytosis using techniques like genetic manipulations, confocal imaging, and biochemical analyses.

Article Abstract

The epidermal growth factor receptor (EGFR), a member of the erythroblastic leukemia viral oncogene homologue (ErbB) receptor tyrosine kinase family, plays key mitogenic signaling roles in development, cellular, and tissue physiology, as well as a myriad of malignancies. EGFR signaling occurs concurrently with ligand-receptor binding and subsequent endocytosis, and its signaling strength and engagement of different downstream signaling components are modulated by its endocytic trafficking itinerary. Understanding the factors and mechanisms that modulate ligand-bound EGFR's endocytic trafficking is therefore important for deciphering its role in pathophysiological processes. Endocytic trafficking of EGFR is regulated by a bunch of Rab small GTPases associated with the endocytic pathway. In this chapter, we describe a suite of relatively standard protocols in dissecting the role of a particular Rab protein in EGFR endocytic trafficking steps/stages. The approach constitutes a combination of genetic/molecular manipulations, followed by confocal imaging and a range of biochemical analyses. We shall mainly focus on Rab31 in our illustrations, but the approaches would be equally applicable to any Rab and its associated regulators/effectors.

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Source
http://dx.doi.org/10.1007/978-1-4939-2309-0_18DOI Listing

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